Canonical Allele Identifier: PA2827772743
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Gly329Val
CA317185
NM_001353952.2:c.986G>T